scispace - formally typeset
S

Stephen J. Smith

Researcher at Allen Institute for Brain Science

Publications -  127
Citations -  22271

Stephen J. Smith is an academic researcher from Allen Institute for Brain Science. The author has contributed to research in topics: Postsynaptic potential & Synapse. The author has an hindex of 59, co-authored 118 publications receiving 20466 citations. Previous affiliations of Stephen J. Smith include Stanford University & Yale University.

Papers
More filters
Journal ArticleDOI

The classical complement cascade mediates CNS synapse elimination.

TL;DR: It is shown that C1q, the initiating protein in the classical complement cascade, is expressed by postnatal neurons in response to immature astrocytes and is localized to synapses throughout the postnatal CNS and retina, supporting a model in which unwanted synapses are tagged by complement for elimination and suggesting that complement-mediated synapse elimination may become aberrantly reactivated in neurodegenerative disease.
Journal ArticleDOI

NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurones

TL;DR: It is directly demonstrated that excitatory amino acids acting at NMDA receptors on spinal cord neurones increase the intracellular Ca2+ activity, measured using the indicator dye arsenazo III, and that this is the result of Ca2- influx through NMDA receptor channels.
Journal ArticleDOI

Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture

TL;DR: A simple and reproducible 3D culture approach for generating a laminated cerebral cortex–like structure, named human cortical spheroids (hCSs), from pluripotent stem cells, which demonstrate that cortical neurons participate in network activity and produce complex synaptic events.
Journal ArticleDOI

Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways

TL;DR: A novel role for astrocytes in mediating synapse elimination in the developing and adult brain is revealed, MEGF10 and MERTK are identified as critical proteins in the synapse remodelling underlying neural circuit refinement, and have important implications for understanding learning and memory as well as neurological disease processes.
Journal ArticleDOI

Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation

TL;DR: It is suggested that dendritic filopodia may actively initiate synaptogenic contacts with nearby axons and thereafter evolve into dendrite spines.